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scGRN-熵:利用单细胞数据和基于基因调控网络的转移熵推断细胞分化轨迹。

scGRN-Entropy: Inferring cell differentiation trajectories using single-cell data and gene regulation network-based transfer entropy.

作者信息

Sun Rui, Cao Wenjie, Li ShengXuan, Jiang Jian, Shi Yazhou, Zhang Bengong

机构信息

School of Mathematical & Physical Sciences, Wuhan Textile University, Wuhan, Hubei, China.

Center for Applied Mathematics and Interdisciplinary Studies, Wuhan Textile University, Wuhan, Hubei, China.

出版信息

PLoS Comput Biol. 2024 Nov 25;20(11):e1012638. doi: 10.1371/journal.pcbi.1012638. eCollection 2024 Nov.

DOI:10.1371/journal.pcbi.1012638
PMID:39585902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11627384/
Abstract

Research on cell differentiation facilitates a deeper understanding of the fundamental processes of life, elucidates the intrinsic mechanisms underlying diseases such as cancer, and advances the development of therapeutics and precision medicine. Existing methods for inferring cell differentiation trajectories from single-cell RNA sequencing (scRNA-seq) data primarily rely on static gene expression data to measure distances between cells and subsequently infer pseudotime trajectories. In this work, we introduce a novel method, scGRN-Entropy, for inferring cell differentiation trajectories and pseudotime from scRNA-seq data. Unlike existing approaches, scGRN-Entropy improves inference accuracy by incorporating dynamic changes in gene regulatory networks (GRN). In scGRN-Entropy, an undirected graph representing state transitions between cells is constructed by integrating both static relationships in gene expression space and dynamic relationships in the GRN space. The edges of the undirected graph are then refined using pseudotime inferred based on cell entropy in the GRN space. Finally, the Minimum Spanning Tree (MST) algorithm is applied to derive the cell differentiation trajectory. We validate the accuracy of scGRN-Entropy on eight different real scRNA-seq datasets, demonstrating its superior performance in inferring cell differentiation trajectories through comparative analysis with existing state-of-the-art methods.

摘要

细胞分化研究有助于更深入地理解生命的基本过程,阐明癌症等疾病的内在机制,并推动治疗学和精准医学的发展。现有的从单细胞RNA测序(scRNA-seq)数据推断细胞分化轨迹的方法主要依靠静态基因表达数据来测量细胞间的距离,进而推断伪时间轨迹。在这项工作中,我们引入了一种新方法scGRN-Entropy,用于从scRNA-seq数据推断细胞分化轨迹和伪时间。与现有方法不同,scGRN-Entropy通过纳入基因调控网络(GRN)中的动态变化来提高推断准确性。在scGRN-Entropy中,通过整合基因表达空间中的静态关系和GRN空间中的动态关系,构建一个表示细胞间状态转换的无向图。然后,基于GRN空间中的细胞熵推断出的伪时间来细化无向图的边。最后,应用最小生成树(MST)算法得出细胞分化轨迹。我们在八个不同的真实scRNA-seq数据集上验证了scGRN-Entropy的准确性,通过与现有最先进方法的对比分析,证明了其在推断细胞分化轨迹方面的卓越性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/c8f91a42fc20/pcbi.1012638.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/420067204a92/pcbi.1012638.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/4a2cd981d614/pcbi.1012638.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/872c8c53c1cd/pcbi.1012638.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/5a6a34dd2f13/pcbi.1012638.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/c8f91a42fc20/pcbi.1012638.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/420067204a92/pcbi.1012638.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/4a2cd981d614/pcbi.1012638.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/872c8c53c1cd/pcbi.1012638.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/5a6a34dd2f13/pcbi.1012638.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f119/11627384/c8f91a42fc20/pcbi.1012638.g005.jpg

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本文引用的文献

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Nat Commun. 2024 Feb 15;15(1):1387. doi: 10.1038/s41467-024-45661-w.
2
A relay velocity model infers cell-dependent RNA velocity.接力速度模型推断细胞依赖的 RNA 速度。
Nat Biotechnol. 2024 Jan;42(1):99-108. doi: 10.1038/s41587-023-01728-5. Epub 2023 Apr 3.
3
scFates: a scalable python package for advanced pseudotime and bifurcation analysis from single-cell data.scFates:一个用于从单细胞数据中进行高级拟时和分支分析的可扩展 Python 包。
Bioinformatics. 2023 Jan 1;39(1). doi: 10.1093/bioinformatics/btac746.
4
UniTVelo: temporally unified RNA velocity reinforces single-cell trajectory inference.UniTVelo:时间统一的 RNA 速度增强了单细胞轨迹推断。
Nat Commun. 2022 Nov 3;13(1):6586. doi: 10.1038/s41467-022-34188-7.
5
spliceJAC: transition genes and state-specific gene regulation from single-cell transcriptome data.拼接 JAC:从单细胞转录组数据中过渡基因和状态特异性基因调控。
Mol Syst Biol. 2022 Nov;18(11):e11176. doi: 10.15252/msb.202211176.
6
Density-based detection of cell transition states to construct disparate and bifurcating trajectories.基于密度的细胞过渡态检测以构建不同和分支轨迹。
Nucleic Acids Res. 2022 Nov 28;50(21):e122. doi: 10.1093/nar/gkac785.
7
Identifying multicellular spatiotemporal organization of cells with SpaceFlow.利用 SpaceFlow 识别细胞的多细胞时空组织。
Nat Commun. 2022 Jul 14;13(1):4076. doi: 10.1038/s41467-022-31739-w.
8
Inference of cell state transitions and cell fate plasticity from single-cell with MARGARET.基于 MARGARET 从单细胞推断细胞状态转变和细胞命运可塑性。
Nucleic Acids Res. 2022 Aug 26;50(15):e86. doi: 10.1093/nar/gkac412.
9
Temporal modelling using single-cell transcriptomics.基于单细胞转录组学的时间建模。
Nat Rev Genet. 2022 Jun;23(6):355-368. doi: 10.1038/s41576-021-00444-7. Epub 2022 Jan 31.
10
VeTra: a tool for trajectory inference based on RNA velocity.VeTra:一种基于RNA速度的轨迹推断工具。
Bioinformatics. 2021 Oct 25;37(20):3509-3513. doi: 10.1093/bioinformatics/btab364.